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  • Patients
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    • Patient information
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  • Reporting obligation
    • Legal framework
    • Cancer registration explained in brief
    • Obligations
    • What needs to be reported?
    • How is reporting done?
    • Online Reporting Platform
  • Statistics and reports
    • Statistics
      • Incidence
      • Mortality
      • Survival
      • Data Quality
    • Cancer monitoring BFS
    • Health reporting on cancer (HRC)
    • Annual reports
    • Cancer Report
  • Publications
  • Data
    • Data availability
    • Data Use regulations (DUR)
    • Data requests

Team

Prof. Dr. med. Claudia Kuehni, director

Ursula Kühnel, executive coordination

PD. Dr. Ben Spycher, statistical consulting

Marina Haller, statistics

Dr. Grit Sommer, head data requests

Alex Junghans, data management

Sophia della Valle, expert tumour coding and data quality

Christina Cinar-Kaufmann, expert registration and process

Maria Hammer, coding and registration

Gabrielle Vautravers Bayram, coding and registration

Mirjam Weiss, registration

  • Organisation
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News

  • International Childhood Cancer Day – ten years of fighting cancer togetherFebruary 15, 2025 - 4:00 am
  • First national health report on cancer highlights the risk of secondary tumorsDecember 10, 2024 - 10:27 am
  • Population information – cancer-registration.chOctober 15, 2024 - 2:46 pm

Publishing details

Published by www.childhoodcancerregistry.ch
Childhood Cancer Registry (ChCR)
Mittelstr. 43
3012 Bern
childhoodcancerregistry.ispm@unibe.ch
Tel: +41 31 684 56 70

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